Evidence map›Paper›PMID 23703909›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2013

A Raman-based endoscopic strategy for multiplexed molecular imaging.

Cristina L Zavaleta, Ellis Garai, Jonathan T C Liu, Steven Sensarn, Michael J Mandella, Dominique Van de Sompel, Shai Friedland, Jacques Van Dam, Christopher H Contag, Sanjiv S Gambhir

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
31.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

95 citing papers in PubMed, 234 citations in OpenAlex.

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35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Cristina L ZavaletaDepartment of Radiology, Stanford University, Stanford, CA 94305, USA.
Ellis Garai
Jonathan T C Liu
Steven Sensarn
Michael J Mandella
Dominique Van de Sompel
Shai Friedland
Jacques Van Dam
Christopher H Contag
Sanjiv S Gambhir
Stanford University · USStony Brook University · USUniversity of Southern California · US

Funding

Stanford Nanocharacterization LaboratoryU54CA119367 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2006 to 2010
$19.8M
Small Animal ImagingP50CA114747 · NCI · STANFORD UNIVERSITY · PI RAO, JIANGHONG · 2005 to 2014
$18.2M
STANFORD CANCER IMAGING TRAINING (SCIT) PROGRAMT32CA009695 · NCI · STANFORD UNIVERSITY · PI BRUCE L DANIEL, Jeremy Dahl · 1993 to 2026
$7.7M
Task Specific Project 2U54CA136465 · NCI · STANFORD UNIVERSITY · PI WENDER, PAUL ANTHONY · 2008 to 2013
$5.3M
NCI NIH HHS P50 CA114747NCI NIH HHS T32 CA009695NCI NIH HHS U54 CA119367NCI NIH HHS U54 CA136465PHS HHS 5-R01-EBB000312
6 · The paper itself

Abstract

Endoscopic imaging is an invaluable diagnostic tool allowing minimally invasive access to tissues deep within the body. It has played a key role in screening colon cancer and is credited with preventing deaths through the detection and removal of precancerous polyps. However, conventional white-light endoscopy offers physicians structural information without the biochemical information that would be advantageous for early detection and is essential for molecular typing. To address this unmet need, we have developed a unique accessory, noncontact, fiber optic-based Raman spectroscopy device that has the potential to provide real-time, multiplexed functional information during routine endoscopy. This device is ideally suited for detection of functionalized surface-enhanced Raman scattering (SERS) nanoparticles as molecular imaging contrast agents. This device was designed for insertion through a clinical endoscope and has the potential to detect and quantify the presence of a multiplexed panel of tumor-targeting SERS nanoparticles. Characterization of the Raman instrument was performed with SERS particles on excised human tissue samples, and it has shown unsurpassed sensitivity and multiplexing capabilities, detecting 326-fM concentrations of SERS nanoparticles and unmixing 10 variations of colocalized SERS nanoparticles. Another unique feature of our noncontact Raman endoscope is that it has been designed for efficient use over a wide range of working distances from 1 to 10 mm. This is necessary to accommodate for imperfect centering during endoscopy and the nonuniform surface topology of human tissue. Using this endoscope as a key part of a multiplexed detection approach could allow endoscopists to distinguish between normal and precancerous tissues rapidly and to identify flat lesions that are otherwise missed.

Indexed as

EndoscopesAdenomatous PolypsColonColonic NeoplasmsColonoscopyEquipment DesignHumansMaleModels, StatisticalNanoparticlesOptical FibersPilot ProjectsPrecancerous ConditionsQuartzScattering, RadiationSensitivity and SpecificityQuartzcolonoscopyoptical

Identifiers

PMID23703909
PMCPMC3690865
OpenAlexW2122296714

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.